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Preparative Work for Target Components at

                          High Purity Levels and High Concentrations











                       Automatic Removal of Non-volatile Salts


                     In the conventional preparative LC, salts derived from the mobile phase are included in the recovered product. With Nexera UFPLC,
                     salts derived from the mobile phase can be removed on the trap column.
                       In the picture below, Ibuprofen was prepared using a solvent containing ammonium chloroacetate, a non-volatile salt. With
                     conventional preparative LC, ammonium chloroacetate precipitated at the same time during evaporation. However, ibuprofen was
                     recovered as a single component with Nexera UFPLC due to the use of a trap column.

                                   mAu
                                 400                                                       Prep LC
                                       Trapping column 1
                                       Trapping column 2   Valerophenone
                                 300
                                       Trapping column 3
                                 200                                            Ammonium Chloroacetate Salts

                                                Ibuprofen                              Nexera UFPLC
                                 100

                                  0
                                   0.0      2.5       5.0       7.5      min
                                      Preparative Chromatogram for Ibuprofen and       Ibuprofen
                                         Analogous Substances (Nexera UFPLC)


                       Concentration and Powdering of Target Ingredients in a Short Period of Time


                     Using Nexera UFPLC, samples are repeatedly injected and the target components are introduced into the same trap column,
                     allowing concentration on the trap column (up to 100 mg capacity). After concentration, the target component is eluted with an
                     organic solvent, allowing recovery of the target component at a high concentration and shortening the time for evaporation.
                       The volume of recovered liquid and the time required for evaporation were measured when 100 mg of the target component,
                     ibuprofen, was puri ed by trap puri cation. Compared to the conventional preparative LC process, the overall time was reduced
                     by 50%.
                                             Comparison of Preparative LC and UFPLC Fractionation
                                                         Fraction vol.  Fraction conc.  Drying time * 1
                                          System
                                                           (mL)        (mg/mL)       (min)
                                      Typical Preparative LC  93.0       1.1         355 * 2
                                      Nexera UFPLC          9.1         11.0         130
                                    *1  Comparison of drying times when a centrifugation enrichment dryer is used
                                    *2  Time for drying the solution (20 mg) collected in one cycle


                              15 min × 5 cycles                      355 min
                       Typical
                    Preparative  Preparative Work                  Powderization                       Total:
                          LC                                                                           430 min
                              15 min × 5 cycles  15 min  130 min
                      Nexera  Preparative Work     Powderization    Total: 220 min
                        UFPLC
                                            Enrichment Purification
                                        Comparison of Procedural Times for Typical Preparative LC and UFPLC


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